The Site Management Associate role involves maintaining systems, managing documents, and streamlining communication in clinical research. Responsibilities include database maintenance, document handling, coordination with external parties and investigative sites, and providing administrative support for project meetings.

The Regional Project Lead is responsible for managing project teams across designated countries, ensuring compliance with industry regulations and project milestones. They prepare status updates, oversee project documentation, handle budgets and contractual negotiations, and supervise team training and performance. Communicating with internal and external stakeholders is essential, as well as managing study audits and ensuring adherence to project timelines.

The Senior SAS Developer will lead clinical database programming services, ensuring the accuracy and consistency of clinical trial data, validating data according to SDTM specifications, and liaising with clients regarding electronic data transfers. The role involves programming, data listing generation, and testing as part of a global Data Management team.

The IT Systems Engineer will evaluate, test, and implement IT infrastructure systems to support PSI's business operations. Responsibilities include maintaining networks, managing setup and configuration of IT systems, optimizing LAN and WAN, managing backups, and training on system processes.

The Senior Data Manager oversees data management activities for large clinical studies, ensuring accuracy in data collection, database locking, and quality control. Responsibilities include training junior team members, communication with clients and vendors, and participating in audits. The role also involves developing SOPs and participating in the design of data collection tools.

The Site Identification Specialist is responsible for developing strategic relationships with clinical research sites, optimizing clinical trial progress, maintaining internal databases, and supporting project teams in site evaluation and identification. They ensure compliance with regulations and assist in study startup activities.

The Senior SAS Developer role involves programming and developing clinical databases, ensuring data quality and consistency, validating clinical trial data, supporting CDISC standards, and liaising with vendors on data transfers.

The Grants Expense Coordinator will ensure timely and accurate payments to physicians and hospitals participating in clinical research. Responsibilities include budgeting, processing payment calculations, communication with various teams, setting up payment databases, and making the payment process transparent through reporting and forecasting.

The Regional Project Lead coordinates and manages project teams across designated regions, ensuring compliance with industry regulations and milestones are met. They oversee project planning, status reporting, training, and the preparation of study documents, while addressing performance issues and maintaining communication within the project team.

As a Project Finance Manager, you will be responsible for budgeting clinical projects, managing project finance information, preparing sponsor contracts, and overseeing timesheet systems. The role requires strong analytical and communication skills, with a focus on delivering timely and accurate financial information throughout project lifecycles.

The Study Startup Specialist I supports site activation processes, feasibility research, budget negotiations, regulatory document collection, and communication with project teams and sites. They maintain tracking systems and supervise Trial Master File maintenance throughout the startup phase.

As a Full Stack Developer, you will architect, develop, and maintain business applications, process user requests for new and existing IT systems, prepare documentation, execute software tests, and track development tasks. You will also be responsible for following development standards and advancing your professional skills in the rapidly evolving tech environment.

As a Study Startup Lead, you will oversee study startup activities, coordinate site agreements, ensure smooth project initiation, monitor activation progress, and analyze startup metrics while managing local project teams.

The Site Management Associate supports clinical research projects by maintaining databases, managing documents, coordinating communication with vendors and investigative sites, and assisting with meeting arrangements. This role requires strong organizational skills and the ability to work independently in a fast-paced environment.

The Site Identification Specialist will develop relationships with clinical research sites to advance clinical trials. Responsibilities include maintaining site databases, communicating with project teams, conducting site evaluations, and ensuring compliance with regulations. The role demands collaboration and strategic planning to identify optimal study sites and address potential issues in project timelines.

The Study Startup Specialist will support the operational processes for site activation in clinical trials, ensuring timely and smooth project startup. Responsibilities include supporting feasibility studies, maintaining project tracking systems, handling site agreements, and facilitating communication among all parties involved in the clinical projects.

As a Junior Programmer, you will develop and maintain client-side applications, translating business needs into functional and visually appealing web applications. Responsibilities include processing user requests, coding in HTML, CSS, JavaScript, and jQuery, ensuring application design consistency, and collaborating on software testing and code reviews.

The Study Startup Assistant will support clinical research teams by managing administrative tasks related to the clinical study startup process, including document management, submissions to authorities, and monitoring project performance metrics in Taiwan.

As a Junior Programmer, you will develop and maintain client-side applications, translating user requests into functional applications. Responsibilities include coding with HTML, CSS, JavaScript, jQuery, and working with C#, .NET, and SQL to integrate with server logic, alongside tracking tasks in Jira and participating in software testing and code reviews.

As a Junior Programmer at PSI, you will develop and maintain client-side applications, process user requests, create user-friendly interfaces, and ensure alignment with existing design concepts. You will work with technologies like HTML, CSS, JavaScript, and C# while participating in code reviews and software testing.